Recombinant SADS-CoV as a vector for porcine epidemic diarrhea vaccine development

猪流行性腹泻病毒 病毒学 生物 重组DNA 维罗细胞 免疫原性 病毒 载体(分子生物学) 冠状病毒 免疫系统 重组病毒 腹泻 抗原 dna疫苗 微生物学 免疫学 医学 免疫 2019年冠状病毒病(COVID-19) 基因 遗传学 病理 传染病(医学专业) 内科学 疾病
作者
Xiaoling Yan,Xiaoli Zhang,Xuefeng Lyu,Yaoyao Zheng,Qianniu Li,Xiaoya Zhao,Jun Fu,Jingyun Ma
出处
期刊:Frontiers in Immunology [Frontiers Media]
卷期号:16: 1633661-1633661
标识
DOI:10.3389/fimmu.2025.1633661
摘要

Introduction Swine acute diarrhea syndrome coronavirus (SADS-CoV) is an emerging porcine enteric coronavirus that can cause diarrhea in piglets younger than 5 days of age. However, infection of pigs older than 5 days of age does not usually result in obvious clinical symptoms. This relative intrinsic safety in older animals prompted us to investigate the potential of SADS-CoV as a viral vector for porcine diarrhea virus vaccines. Methods We utilized Gibson assembly to clone the SADS-CoV sequence into an artificial bacterial chromosome (BAC) vector. Further manipulation was carried out by recombineering to generate four attenuated recombinant SADS-CoV strains expressing a PEDV protective antigen fused with peptides that target immune cells. Subsequently, the biological characteristics and immunogenic efficacy of these four recombinant strains were systematically assessed through in vitro cell models and in vivo animal challenge experiments. Results and discussion The recombinant viruses exhibited a proliferation profile similar to that of the wild-type virus in Vero cells, maintained stable cytopathic effects, retained the exogenous sequences for up to 20 passages, and consistently expressed the PEDV antigen fusion protein. Immunizing pregnant sows with these recombinant viruses effectively enhanced both cellular and mucosal immune responses and provided significant clinical protection against PEDV to their offspring. This study not only generated a vaccine candidate for PEDV but also established a pipeline for using the SADS-CoV as a vector for vaccine development.
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